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U.S. Department of Health and Human Services

Enforcement Report - Week of September 25, 2013

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Product Detail

Product Description Source Plasma
Recall Number B-2313-13
Classification Class II
Code Info 0530546029, 0530545681, 0530542822, 0530542328, 0530540867, 0530540564, 0530539531, 0530539185, 0530537708, 0530536769, 0530536312, 0530533622, 0530533283, 0530532387, 0530531990, 0530530965, 0530530556, 0530529630, 0530529182, 0530528280, 0530526014, 0530525450, 0530521176, and 0530520099.
Product Distributed Qty 24 units
Reason For Recall Blood products, collected from a donor whose physical was overdue, were distributed.

Event Detail

Event Id 49951
Product Type Biologics
Status Terminated
Recalling Firm ZLB Bioplasma, Inc.
City Lexington
State KY
Country US
Voluntary / Mandated Voluntary: Firm Initiated
Recall Initiation Date 2009-08-22
Initial Firm Notification of Consignee or Public Letter
Distribution Pattern IL, Germany, and Switzerland.
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